| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:178213998-178214233 | Common:1; Rare:45 | ||||
| chr5:178217375-178217565 | Common:7; Rare:29 | ||||
| chr5:179832938-179833139 | Common:3; Rare:93; Clinvar:6; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr5:179833149-179833590 | Common:14; Rare:146; Clinvar:3; Clinvar (benign):8 | ||||
| chr5:180830827-180831041 | Common:1; Rare:65 | ||||
| chr5:180831564-180831679 | Common:2; Rare:49 | ||||
| chr5:180930611-180930668 | Rare:10 | ||||
| chr5:180936941-180937042 | Common:1; Rare:15 | ||||
| chr5:180996687-180996976 | Common:2; Rare:24 | ||||
| chr6:2272653-2272842 | Common:2; Rare:26 | ||||
| chr6:2833887-2834139 | Common:2; Rare:51 | ||||
| chr6:3104142-3104308 | Common:1; Rare:37 | ||||
| chr6:3285597-3285691 | Common:2; Rare:19 | ||||
| chr6:3313166-3313427 | Rare:39 | ||||
| chr6:3317906-3317967 | Rare:12 |